4.8 Article

A Bimetallic Zn/Fe Polyphthalocyanine-Derived Single-Atom Fe-N-4 Catalytic Site:A Superior Trifunctional Catalyst for Overall Water Splitting and Zn-Air Batteries

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 57, Issue 28, Pages 8614-8618

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201804349

Keywords

electrochemistry; EXAFS; N-doped porous carbon; polymerization; pyrolysis

Funding

  1. National Key R&D Program of China [2017YFA0700101, 2016YFA0202801]
  2. National Natural Science Foundation of China [21573119, 21590792, 21521091, 21390393, U1463202]
  3. China Postdoctoral Science Foundation [2017M610076]
  4. Beijing Natural Science Foundation [2184104]

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Developing an efficient single-atom material (SAM) synthesis and exploring the energy-related catalytic reaction are important but still challenging. A polymerization-pyrolysis-evaporation (PPE) strategy was developed to synthesize N-doped porous carbon (NPC) with anchored atomically dispersed Fe-N-4 catalytic sites. This material was derived from predesigned bimetallic Zn/Fe polyphthalocyanine. Experiments and calculations demonstrate the formed Fe-N-4 site exhibits superior trifunctional electrocatalytic performance for oxygen reduction, oxygen evolution, and hydrogen evolution reactions. In overall water splitting and rechargeable Zn-air battery devices containing the Fe-N-4 SAs/NPC catalyst, it exhibits high efficiency and extraordinary stability. This current PPE method is a general strategy for preparing M SAs/NPC (M=Co, Ni, Mn), bringing new perspectives for designing various SAMs for catalytic application.

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